论文部分内容阅读
目的探讨分析前待检标本的质量管理,分析原因降低待检标本不合格率。方法对2015年临检中心接受医院各科室送检标本数量、不合格标本的数量、拒收原因、不合格比例进行分析。结果 2015年临检中心接受医院各科室标本326622份,不合格标本总数为457份(0.14%)。不合格标本中占比较高的是标本凝块123例,占26.91%;其次是标本量少20.35%、标本容器不符17.07%。结论采用对临床医生、护理人员培训、与护士长沟通等方法可以降低待检标本不合格率,提高分析前质量管理。
Objective To explore the quality control of the specimens to be examined before analysis and analyze the reasons to reduce the failure rate of specimens to be examined. Methods The clinical laboratory in 2015 accepted the number of specimens submitted to the hospital, the number of non-conforming specimens, the reasons for rejection, and the unqualified proportions. Results The 2015 clinical examination center received 326,622 samples from all departments and hospitals, with a total of 457 (0.14%) unqualified samples. Among the unqualified samples, 123 samples were clotted, accounting for 26.91%, followed by 20.35% less specimens and 17.07% specimens. Conclusion The methods of training clinicians, nurses and communicating with nurses can reduce the failure rate of samples to be inspected and improve the quality management before analysis.